A novel therapeutic strategy: the significance of exosomal miRNAs in acute myeloid leukemia

被引:3
|
作者
Salehi, Ali [1 ]
机构
[1] Islamic Azad Univ, Dept Cellular & Mol Biol, Tehran Med Branch, Facul New Sci & Technol, Tehran, Iran
关键词
Acute myeloid leukemia; MiRNA; Exosome; Pathogenesis; Microenvironment; MESENCHYMAL STROMAL CELLS; MINIMAL RESIDUAL DISEASE; BONE-MARROW NICHE; STEM-CELLS; TUMOR-SUPPRESSOR; EXTRACELLULAR VESICLES; MICRORNA SIGNATURES; MEDIATED TRANSFER; DOWN-REGULATION; EMERGING ROLES;
D O I
10.1007/s12032-023-02286-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Acute myeloid leukemia (AML) is a fast-growing blood cancer that interferes with the normal growth of blood cells in the bone marrow and blood. It is characterized by its unpredictable outlook and high death rate. The main treatment for AML is chemotherapy, but this often results in drug resistance and the possibility of the disease returning. For this reason, new biomarkers are necessary to diagnose, predict, and treat this disease. Research has demonstrated that cells responsible for AML release exosomes that interact with the disease's microenvironment. These exosomes have significant roles in promoting leukemia growth, suppressing normal hematopoiesis, facilitating angiogenesis, and contributing to drug resistance in AML. Further investigations have shown that these exosomes contain miRNAs, which are transferred to target cells and have functional roles. Biomarkers are utilized to assess various aspects of tumor cell behavior, including proliferation, apoptosis, angiogenesis, changes in the microenvironment, transfer of drug resistance, and stability in serum and blood plasma. In this research, we showed that exosomal miRNAs and exosomes have the potential to be used as indicators for detecting various phases of AML and can aid in its medical treatment. Furthermore, they can be specifically targeted for therapeutic purposes in addressing this condition.
引用
收藏
页数:26
相关论文
共 50 条
  • [1] A novel therapeutic strategy: the significance of exosomal miRNAs in acute myeloid leukemia
    Ali Salehi
    Medical Oncology, 41
  • [2] Induction of apoptosis by obovatol as a novel therapeutic strategy for acute myeloid leukemia
    Kim, Hyeng-Soo
    Lim, Ga Young
    Hwang, Junmo
    Ryoo, Zae Young
    Huh, Tae-Lin
    Lee, Sanggyu
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2014, 34 (06) : 1675 - 1680
  • [3] miRNAs in acute myeloid leukemia
    Liao, Qiong
    Wang, Bingping
    Li, Xia
    Jiang, Guosheng
    ONCOTARGET, 2017, 8 (02) : 3666 - 3682
  • [4] Role of exosomal miRNAs and macrophage polarization in gastric cancer: A novel therapeutic strategy
    Zhang, Yun
    Wang, Baozhen
    Chen, Jing
    Li, Tao
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2025, 990
  • [5] Novel therapeutic agents in acute myeloid leukemia
    Stone, Richard M.
    EXPERIMENTAL HEMATOLOGY, 2007, 35 (04) : 163 - 166
  • [6] NOVEL THERAPEUTIC TARGETS IN ACUTE MYELOID LEUKEMIA
    Martelli, M. P.
    Falini, B.
    HAEMATOLOGICA, 2017, 102 : 192 - 195
  • [7] Risk Adapted Therapeutic Strategy of Acute Myeloid Leukemia
    Mohty, Razan
    Massoud, Radwan
    Chakhachiro, Zaher
    Mahfouz, Rami
    Nassif, Samer
    Elcheikh, Jean
    Bazarbachi, Ali
    BLOOD, 2019, 134
  • [8] Targeting Autophagy As a Therapeutic Strategy in Acute Myeloid Leukemia
    Nourkeyhani, Houman
    Jason, Den Haese P.
    Scott, Portwood
    Hanekamp, Diana
    Johnson, Megan
    Wang, Eunice S.
    BLOOD, 2016, 128 (22)
  • [9] A novel therapeutic strategy for alleviating atrial remodeling by targeting exosomal miRNAs in atrial fibrillation
    Hao, Hongting
    Dai, Chenguang
    Han, Xuejie
    Li, Yue
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2022, 1869 (12):
  • [10] Targeting the Mammalian Mitochondrial Clpp (mClpP) As a Novel Therapeutic Strategy for Acute Myeloid Leukemia
    Cole, Alicia
    Wang, Zezhou
    Mattson, Rachel
    Hurren, Rose
    Lin, Fengshu
    Gronda, Marcela
    Maclean, Neil
    Isaac, Methvin
    Leung, Elisa
    Babu, Mohan
    Sukhai, Mahadeo A.
    Houry, Walid A.
    Schimmer, Aaron D.
    BLOOD, 2012, 120 (21)